The C-nucleoside 2'-deoxypseudouridine, in contrast to dU, forms stable C:pseudoU-A triplets.
Classic 2'-OTBDMS phosphoramidite for incorporation of U into a synthetic oligonucleotide.
Phosphoramidite for the efficient incorporation of a fluorescent deoxycytidine analogue into oligonucleotides.
Phosphoramidite for incorporation of a 2'-O-methyl modified ribo-C nucleobase within an oligonucleotide
Phosphoramidite used to incorporate a 5'-capped dT in an oligonucleotide.
Phosphoramidite for incorporation of an (otherwise unmodified) reverse (5’ to 3’) dT nucleobase within an oligonucleotide.
Phosphoramidite to incorporate an amino functionality on deoxyuridine, for post-synthetic conjugation.
Fluorous-tagged nucleoside useful for the purification of oligonucleotides.
Half of a novel base pair (with dNaM) that achieves pair recognition through hydrophobic interactions.
Phosphoramidite for incorporation of a 2'-O-methyl modified ribo-G nucleobase within an oligonucleotide
| Europe, Middle East, and Africa | |
|---|---|
| UK | +44 1992 470 757 |
| Germany | +49 30 1663 54600 |
| North America, Latin America | |
| Wisconsin, USA | +1 888 575 9695 |
| Asia Pacific | |
| China | +8621-22509000 |
| Singapore | +65 6734 4800 |
